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D Cohn

Showing results (331-340 of 379) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin systemPeter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine|March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expressionEleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Environmental Health Perspectives|August 17, 2012
The Head-off Environmental Asthma in Louisiana (HEAL) study--methods and study populationPatricia C Chulada, Suzanne Kennedy, Mosanda M Mvula, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature|July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier geneDwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One|November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrelsEva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
Environmental Health Perspectives|August 17, 2012
Implementation of evidence-based asthma interventions in post-Katrina New Orleans: the Head-off Environmental Asthma in Louisiana (HEAL) studyHerman Mitchell, Richard D Cohn, Jeremy Wildfire, et al.
Contemporary Clinical Trials|March 24, 2017
Rationale and study protocol for the Patient-Centered Outcome Aid (PCOA) randomized controlled trial: A personalized decision tool for newly diagnosed ovarian cancer patientsL Wenzel, D Mukamel, K Osann, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Pageof 38

Showing results (331-340 of 379) with videos related to

Sort By:
Pageof 38
Proceedings of the National Academy of Sciences of the United States of America|August 20, 2011
Identification and characterization of a functional mitochondrial angiotensin systemPeter M Abadir, D Brian Foster, Michael Crow, et al.
EMBO Molecular Medicine|March 16, 2021
Targeted genome editing in vivo corrects a Dmd duplication restoring wild-type dystrophin expressionEleonora Maino, Daria Wojtal, Sonia L Evagelou, et al.
Environmental Health Perspectives|August 17, 2012
The Head-off Environmental Asthma in Louisiana (HEAL) study--methods and study populationPatricia C Chulada, Suzanne Kennedy, Mosanda M Mvula, et al.
Pediatrics|July 4, 2006
Intracranial hemorrhage as the initial manifestation of a congenital disorder of glycosylationRonald D Cohn, Erik Eklund, Amanda L Bergner, et al.
Nature Communications|August 4, 2015
Clinically relevant copy number variations detected in cerebral palsyMaryam Oskoui, Matthew J Gazzellone, Bhooma Thiruvahindrapuram, et al.
Nature|July 26, 2019
A mutation-independent approach for muscular dystrophy via upregulation of a modifier geneDwi U Kemaladewi, Prabhpreet S Bassi, Steven Erwood, et al.
Plos One|November 17, 2012
Impaired skeletal muscle regeneration in the absence of fibrosis during hibernation in 13-lined ground squirrelsEva Andres-Mateos, Rebeca Mejias, Arshia Soleimani, et al.
Environmental Health Perspectives|August 17, 2012
Implementation of evidence-based asthma interventions in post-Katrina New Orleans: the Head-off Environmental Asthma in Louisiana (HEAL) studyHerman Mitchell, Richard D Cohn, Jeremy Wildfire, et al.
Contemporary Clinical Trials|March 24, 2017
Rationale and study protocol for the Patient-Centered Outcome Aid (PCOA) randomized controlled trial: A personalized decision tool for newly diagnosed ovarian cancer patientsL Wenzel, D Mukamel, K Osann, et al.
BMC Genomics|April 30, 2015
Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M SyndromeChristian R Marshall, Sandra A Farrell, Donna Cushing, et al.
Pageof 38